Gelatinase expression in pulmonary arteries during experimental pulmonary hypertension

被引:88
作者
Frisdal, E
Gest, V
Vieillard-Baron, A
Levame, M
Lepetit, H
Eddahibi, S
Lafuma, C
Harf, A
Adnot, S
d'Ortho, MP
机构
[1] Fac Med Creteil, Unite INSERM U492, F-94010 Creteil, France
[2] Hop Ambroise Pare AP HP, Serv Reanimat Med, Boulogne, France
[3] Hop Henri Mondor AP HP, Serv Physiol Explorat Fonct, Creteil, France
关键词
extracellular matrix; hypoxia; matrix metalloproteinase; monocrotaline tissue inhibitor of metalloproteinase;
D O I
10.1183/09031936.01.00084601
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Structural remodelling of pulmonary vessels is an important feature of pulmonary hypertension (PH), which reflects distal artery muscularization and matrix remodelling. The matrix metalloproteinases (MMPs) are involved in extracellular matrix turnover and hence, in smooth muscle cell migration and endothelial cell migration and proliferation. Among the MMPs, gelatinases (MMP-2 and MMP-9) can degrade basement membrane components and promote cell proliferation and migration. This study evaluated gelatinases in pulmonary vessels during progressive PH in two rat models: exposure to hypoxia or monocrotaline. Zymography of tissue homogenates revealed an association of progression of hypoxic PH with a time-dependent increase in gelatinase MMP-2 activity, specific to pulmonary vessels. Increased MMP-2 activity was also found 30 days postmonocrotaline. Reverse transcription polymerase chain reaction demonstrated upregulation of MMP-2 messenger ribonucleic acid. Immunolocalization showed MMP-2 throughout the pulmonary vasculature, from the trunk to the distal vessels, with strong staining of the intima, media and adventitia. MMP-2 was found in its active form and gelatinolytic activity was correlated to PH severity. Activity localization by in situ zymography corroborated with the immunolocalization findings. In conclusion, the authors demonstrated that matrix metalloproteinase-2 activity is increased in pulmonary vessels during progression of pulmonary hypertension, probably as a result of involvement in the matrix turnover associated with vascular remodelling during pulmonary hypertension.
引用
收藏
页码:838 / 845
页数:8
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